Background: Clostridium difficile infection (CDI) incidence, severity and mortality have been increasing over the past decade. Since 1999, CDI discharge diagnosis rates have increased in Illinois. The restriction endonuclease analysis (REA) type BI and North American Pulsed Field Type I (NAP1) strain has been identified in the Chicago area.
Objective: To describe incident CDI cases in Chicago healthcare institutions (HCIs) and assess infection control and laboratory practices.
Methods: A standardized questionnaire was completed for each CDI incident case during February 2009, defined by clinical symptoms and either the first positive C. difficile assay or more than 8 weeks since the last positive test or pseudomembranous colitis (PMC). Clinical and epidemiologic information was collected for each case-patient. Toxin-positive stools of incident cases were characterized to determine strain type. 26 HCIs completed infection control and 23 facilities completed laboratory practice surveys.
Results: HCIs
completed questionnaires for 267 incident case-patients at 27
institutions. Case-patient classifications according to standardized
surveillance definitions are presented in the Table. 38 (14%) of incident
case-patients had severe CDI defined by admission to intensive care, need for
colectomy within 30 days of CDI diagnosis, or death with CDI. Bowel surgery was
required in 6 (16%) of 38 patients with severe disease and 7 (18%) of 38
patients were found to have PMC on endoscopy or on pathologic specimens. 20
(7%) of incident case-patients died. 138 stool specimens from incident
case-patients were typed, of which 61% demonstrated the BI/NAP1 strain.
Individual HCI rates were defined as the number of incident cases of CDI with
symptom onset after 3 days in the hospital per 10,000 patient-days during
February 2009. For those participating hospitals with CDI incident
case-patients during the investigation period, rates ranged from 2-7 case
patients per 10,000 patient days. Of those hospitals with a hand hygiene
policy when caring for patients with CDI, 65% required the use of soap and
water while 35% allowed alcohol hand gel or soap and water. 35% of
hospitals performed terminal cleaning with bleach in rooms previously occupied by
patients with CDI, while 23% performed daily cleaning with a bleach containing
product for rooms of patients with CDI. The majority of HCIs detected CDI by
the EIA for toxin A and B. Providers sent a median of 1 diagnostic test
for CDI (range 1-7 tests) per patient.
Conclusions: CDI infection control practices varied between institutions
surveyed. CDI rates were within the expected range, but caused severe
disease among 14% of case-patients and 7% mortality during the one month
surveillance period. The BI/NAP1 strain has become the dominant type causing
CDI in the Chicago-area.